1-morpholino-1-cyano-0-carbamoyl-formoximes

ABSTRACT

New basically substituted 1-cyano-0-carbamoyl-formoximes are described as insecticides, acaricides and nematocides, which are distinguished from known carbamoyl-oximes by pronounced systemic insecticidal, acaricidal and nematocidal action. A typical compound is 1-diethylamino-0-(N&#39;&#39;-methylcarbamoyl)-formoxime. Processes for the production of these compounds are described as well as pesticidal compositions containing these compounds as active substances.

[ 1 June 28, 1974 l-MORPHOLINO-l-CYANO-O-CARBAM- OYL-FORMOXIMES Inventors: I-Ians Ulrich Brechbuhler, Basel;

Kurt Gubler, Riehen, both of Switzerland Assignees Ciba-Geigy Corporation, Ardsley,

Filed: Apr. 13, 1972 Appl. No.: 243,820

Related U.S. Application Data Division of Ser. No. 844.163, July 23, 1969, Pat. No. 3,673,236.

U.S. Cl 260/247.2 A Int. Cl C07d 87/42 Field of Search 260/2472 A, 465.4

References Cited I FOREIGN PATENTS OR APPLICATIONS 9/1967 France 260/4654 Primary Examiner-Dona1d G. Daus Assistant Examiner-Ralph D. McCloud Attorney, Agent, or Firm-Harry Falber; Frederick H. Rabin [57] ABSTRACT New basically substituted I-cyano-O-carbamoylformoximes are described as insecticides, acaricides and nematocides, which are distinguished from known carbamoyl-oximes by pronounced systemic insecticidal, acaricidal and nematocidal action. A typical compound is 1-diethyIamino-O-(N'-methy1carbamoyl)- formoxime. Processes for the production of these compounds are described as well as pesticidal compositions containing these compounds as active substances.

1 Claim, No Drawings l-MORPHOLINO-l-CYANO-ll-CARBAMOYL- FORMOXIMES This is a division of application Ser. No. 844,163, filed on July 23, 1969, now US. Pat. No. 3,673,236.

DETAILED DESCRIPTION The present invention concerns new carbamoylformoximes, namely l-cyano-O-carbamoylformoximes having a basic group in l-position, process for the production thereof, pesticidal agents containing these new compounds as active substance, as well as methods for the control of pests using the new active substances or agents containing them.

In the South African Pat. No. 66/6759, a number of carbamoyl-oximes of aliphatic aldehydes have already been suggested as insecticidal, acaricidal and nematocidal active substances. In French Pat. No. 1,498,899 l-cyano-l-alkylthio-O-carbamoyl-formoximes, among others, are described therein. This group of active substances, however does not possess any or only insufficient systemic insecticidal properties. Individual members of this group are, moreover, phytotoxic and toxic for warm-blooded animals.

The compounds of the present invention are basically substituted l-cyano-O-carbamoyl-formoximes of the Formula I:

R1 N /Ra N- =NOCON wherein R represents hydrogen, a substituted or unsubstituted lower alkyl radical with one to five carbon atoms,

R represents a lower alkyl radical with one to five carbon atoms, a cycloalkyl radical with three to six carbon atoms, the phenyl radical, the tetrahydrofuryl radical, or

R and R together with the adjacent nitrogen ato represent a or 6-membered-heterocyclic radical,

R represents hydrogen or a lower alkyl radical with one to five carbon atoms and R represents a lower alkyl or alkenyl radical with one to five carbon atoms or two to four carbon atoms, respectively.

Examples of lower alkyl radicals represented by R to R having one to five carbon atoms are methyl, ethyl, n-propyl, isopropyl, n-butyl, tert-butyl, isobutyl and pentyl radicals. Examples of lower alkenyl radicals R are the allyl, methallyl or propenyl radical. Cycloalkyl radicals R arepreferably monocyclic radicals such as cyclopropyl, l-methylcyclopropyl, cyclo'butyl, cyclopentyl and cyclohexyl. Substituted alkyl radicals contain, for example, the following substituents: hydroxy, halogen, lower alkoxy, alkylthio, alkylamino, dialkylamino, whereby alkyl always represents lower alkyl of from 1 to 5 carbon atoms.

A 5- or 6-membered heterocyclic radical formed by R, and R and the adjacent nitrogen atom is preferably saturated and can contain other hetero atoms such as anothernitrogen atom or oxygen atom. These heterocyclic radicals can also contain substituents such as lower alkyl, lower alkoxycarbonyl, etc. Preferred heterocyclic radicals are: the piperidino, piperazino, 4-

methylpiperazino, 4-alkoxycarbonyl-piperazino or the morpholino radical.

The novel l-cyano-O-carhamoyl-formoximcs of the Formula I are produced according to the invention by 5 reacting a l-cyanoformoxime of the Formula 11:

NJJ=NOH R2 (II) either a. with an isocyanate of the Formula 111:

, R NCO (III) or b. with a carbamic acid halide of the Formula IV:

Ha1CN ll wherein Hal represents chlorine or bromine,

c. with the components forming the carbamic acid halide of Formula IV, namely with phosgene and an amine of the Formula V:

preferably in the presence of an acid-binding agent and a solvent or diluent which is inert towards the reaction components. In the Formulas II to V, the symbols-R to K, have the meanings given for Formula I.

For the production of the novel l-cyano-O-carbamoyl-formoximes of Formula I in which R represents hydrogen, a mixture of an isocyanate of Formula 111 and an N-mono-alkyl-carbamic acid halide of the formula can also be used.

The reactions according to the invention are performed in the presence of acid-binding agents such as inorganic bases, e.g. hydroxides, oxides and carbonates of alkali and alkaline earth metals, and organic nitrogen bases, for example tertiary amines such as pyridine, triethylamine, triethylene-diamine, etc., as well as organotin compounds. The reactions are carried out in the presence of solvents and diluents which are inert towards the reaction components, e.g. in ethers and ether-type compounds such as diethylether, propyl ethers, dioxane; ketones such as acetone, methylethyl ketone; amides such as N,N-alkylated carboxylic acid amides; in halogenated hydrocarbons or aliphatic and aromatic hydrocarbons. The novel carbamoyl oximes are obtained according to the invention in good to very good yields. They are soluble in the usual organic solvents and water and are stable. Some of the starting materials of Formula 11 used for the reactions according to the invention are known. The compounds which have not previously been described can be obtained according to the method described by W. Steinkopf et a1., [.l.pr.Chemie (2), 83, 453-470 (1911)], by reacting l-chloro-l-cyano-formoxime with primary and secondary amines.

lt is known that oximes can exist in two stereoisomeric forms, the synand the anti-form. The 1- cyano-O-carbamoyl-formoximes of Formula 1 can also exist in these two forms. For this reason the term lcyano-O-carbamoyl-formoximes of Formula 1 should be understood to represent both of these stereoisomeric forms.

The following examples illustrate the process according to the invention. The temperatures are given in degrees Centigrade and all parts and percentages are by weight unless otherwise specified.

EXAMPLE 1 a. 200 ml of a 33 percent solution of dimethyl amine in absolute ethanol are added to 500 ml of dioxane and then 24 g of l-chloro-l-cyano-formoxime in 100 ml of absolute dioxane are added dropwise with vigorous stirring under an atmosphere of nitrogen. The temperature rises to 40 and a precipitate of dimethylaminehydrochloride is formed. Stirring is continued for 16 hours at room temperature and finally for 2 hours at 60. The solvents are removed by suction under vacuum, the residue is dissolved in a small volume of water, acidified (pH 3-4) with phosphoric acid and extracted with diethyl ether. The ethereal extracts are dried with anhydrous sodium sulfate, and the ether is removed under vacuum. In this manner, 21.4 g of l-dimethylamino-lcyano-formoxime are obtained as brownish crystals having a melting point of 1 12.

b. 5.3 g of 1-dimethylamino-l-cyano-formoxime are dissolved in 50 ml of dioxane, treated with 0.25 ml of triethyl amine, and 7.5 ml of methylisocyanate are added thereto. This mixture is kept for 16 hours at 40-50. After cooling, the dioxane is removed under vacuum and the residue is recrystallized from ethanol. In this manner, 6.9 g of white crystals (m.p. 114l 17) of 1-dimethylamino-1-cyano-O-(N'-methylcarbamoyl)-formoxime are obtained. The mother liquor yields a further 4.5 g, m.p. 112-115.

EXAMPLE 2 EXAMPLE 3 9.6 g of a 50 percent by weight suspension of sodium hydride in paraffin oil are diluted under nitrogen atmosphere with 100 m1 of dry tetrahydrofuran. A solution of 31 g of morpholino-l-cyano-formoxime in 200 ml of dry tetrahydrofuran is added dropwise at room temperature with stirring vigorously to this suspension. Stirring is continued at 35 40 for minutes. This mixture is then added in small portions at O-5'to a stirred solution of 39.6 g of phosgene in 400 m1 of dry ether.

Stirring is continued at room temperature for 30 minutes. The excess of phosgene is then removed in vacuo. A solution of 22.5 g of dimethylamine in ml of dry tetrahydrofuran is then added dropwise at room temperature and the whole is. stirred for 16 hours at room temperature. The reaction mixture is then heated to 60 for 1 hour, the solution is filtered after cooling and the solvent is removed in vacuo.

The residue is washed with hexane in order to remove the paraffin oil and then recrystallized from a water/ethanol mixture. Thus l-morpholino-l-cyano-O- '(N'-dimethyl-carbamoyl)-formoxime melting at -121 is obtained.

The following compounds of Formula 1 were produced-analogously to the processes described in the Examples:

l-morpholinol -cyano-O-( N '-dimethylcarbamoyl)-formoxime Melting Compounds point l-diethyluminol -cyano-O-( N -dimethylcarbamoyl formoxime oil l-di-n-propylaminol -cyano-O-( N '-methylcarbamoyl formoxime oil 'lanilinol -cyano-O-(N'-mcthylcarbamoyl )-lormoximc 172-1 74 l-piperidino- 1 -cyano-O-(N '-mcthylcarbamoyl Hormoxime I 54 l-piperazinol cyano-O-(N -methylcarbamoyl )-formoxime 202 l-(4methyl-piperazino)-1-cyanoO-(N-methylcar bamoyl)-formoxime 82 l-(4-ethoxycarbonyl-piperazino 1 -cyano-( N -methylcarbamoyU-formoxime 105 l-(4-e-thoxycarbonyl-piperazino)-1-eyano-0-(N-dimethylcarbamoyl )-formoxime 137 1 -dimethylaminol -cyano-O-(N -ethylcarbamoyl formoxime 81 l-dimethylamino-l -cyano O-(N '-isopropylearbamoyl formoxime 99 l-dimethylaminol -cyano-O-( N 'allylcarbamoyl)-tormoxime 86 l-dimethylaminol -cyano-O-( N -n-propylcarbamoyl)- formoxime 74 l-morpholinol -cyano-O-(N '-ethylcarbamoyl )-formoxime paste l-diethylaminol -cyano-O-( N '-etliylcarbamoyl)-formoxime oil l-tetrahydrofurfurylamino-O-(N 'methylcarbamoyl formoxime 121-122 The production of pesticidal agents according to the invention is performed in a known manner by intimate mixing and grinding of active substances of the general Formula I together with suitable carriers, optionally with the addition of dispersing agents, absorbents, or solvents, which are inert towards the active substances. The novel active substances can be prepared in the following forms:

solid preparations: dusts, scattering agents, granulates, (coated granula'tes, impregnated granulates and homogeneous granulates);

water-dispersible concentrates of the active substance: wettable powders, pastes, emulsions;

liquid preparations: solutions, aerosols.

The concentration of active substance in these preparations is from 0.01 to 80 percent. Other biocidally active substances or agents can be admixed with the agents described according to the invention. Thus, in

addition to the said active substances of the general Formula 1, the new agents may contain, for example, other insecticides, fungicides, bactericides, fungistatic and bacteriostatic substances or other nematocides in order to broaden the range of action. The agents according to the invention may also contain plant fertilizers, trace elements, etc.

The novel active substances are used for soil disinfection in the form of solid or liquid agents. For soil disinfection, those agents which assure an even distribution of the active substance throughout a layer of soil to cm deep are especially favorable. The method and form of application are, in particular, dependent upon The following ingredients are used to produce (a) a 10 percent and (b) a 2 percent dust:

a. 10 parts of l-n-butylamino-l-cyano-O-(N'- methylcarbamoyl)-formoxime,

5 parts of highly dispersed silicic acid,

parts of talcum;

b. 2 parts of l-morpholino-l-cyano-O-(N- dimethylcarbamoyl)-formoxime,

1. part of highly dispersed silicic acid,

97 parts of talcum.

The active substances are mixed and ground with the carriers. The dusts obtained are used, e.g., for the control of cockroaches and ants, etc.'in buildings, and also for plant protection.

Granulate The following ingredients are used to produce a 5% granulate:

5 parts of isopropylamino-1-cyano-O-(N'-methylcarbamoyl)-formoxime,

0.25 part of epichlorohydrin,

0.25 part of octaethyleneglycol ether,

3.50 parts of polyethyleneglycol of a molecular weight of about 400,

91 parts of kaolin (particle size 0.3-0.8 mm).

The active ingredient is mixed with epichlorohydrin and then dissolved in 6 parts of acetone. and the polyethyleneglycol and octaethyleneglycol ether are added thereto. The solution obtained is sprayed onto kaolin and then the acetone is evaporated in vacuo. The granulate obtained is suitable for the protection of plants and stored goods.

Wettable powder For the production of a 50 percent [(a) and (b)], a 25 percent [(c)], and a 10% [(d)] wettable powder, the following components are used:

a. 50 parts of .l-dimethylamino-l-cyano-O-(N'- methylcarbamoyl)-formoxime,

5 parts of naphthalene sulfonic acid/benzene sul' fonic acid/formaldehyde condensation product,

5 parts of nonylphenyl sulfonate,

5 parts of Champagne chalk,

20 parts of silicic acid,

7 15 parts of kaolin;

b. 50 parts of l-diethylamino-l-cyano-O-(N- dimethylcarbamoyl)-formoxime,

parts of nonylphenyl sulfonate,

parts of calcium lignin sulfonate,

1 part of Champagne chalk/hydroxyethyl cellulose mixture (1:1),

20 parts of silicic acid, 14 parts of kaolin;

25 parts of l-n-propylamino-l-cyano-O-(N- methylcarbamoyl)-formoxime, 5 parts of sodium oleyl methyl tauride, 2.5 parts of naphthalene sulfonic acid/formalde hyde condensation product, 0.5 part of carboxymethyl cellulose, 5 parts of neutral potassium-aluminium silicate, 62 parts of kaolin;

10 parts of l-n-butylamino-l-cyano-O-(N'- methylcarbamoyl)-formoxime, 3 parts of a mixture of the sodium salts of saturated fatty alcohol sulfates,

5 parts of naphthalene sulfonic acid/formaldehyde condensationproduct, 82 parts of kaolin.

The active ingredients are intimately mixed with the additives in suitable mixers and ground in mills and rollers. Wettable powders are obtained which can be diluted with water to form suspensions of any desired concentration. Such suspensions are used primarily in plant protection for the control of biting and sucking insects.

Paste The following ingredients are used to produce a 45 percent paste:

45 parts of l-diethylaminol -cyano-O-( N methylcarbamoyl)-formoxime,

5 parts of sodium aluminium silicate parts of cetyl octaethylene glycol ether 2 parts of spindle oil,

10 parts of polyethyleneglycol of a molecular weight of about 400,

23 parts of water.

The active ingredient is intimately mixed and ground with the additives in apparatus suitable therefor. A paste is obtained from which, by dilution with water, suspensions of any concentration desired can be produced. These suspensions are suitable for the control of insects in plant protection.

Emulsion To produce a 10 percent emulsion concentrate,

10 parts of l-morpholino-l-cyano-O-(N'-methylcarbamoyl)-formoxime,

55 parts of xylene,

32 parts of dimethyl formamide and 3 parts of an emulsifying agent consisting of nonylphenyl decaethyleneglycol and calcium nonylphenylsulfonate (weight ratio about 1:1) are mixed together. This concentrate can be diluted with water to form emulsions having concentrations suitable for the protection of plants and stored goods.

Spray a. 1 part of 1-methylamino-1-cyano-O (N'- methylcarbamoyl)-formoxime are dissolved in 99 parts of water;

b. 2 parts of l-dimethylamino-l-cyano-O-(N- methylcarbamoyl)-formoxime are dissolved in 10 parts of xylene and 88 parts of petroleum;

c. 2 parts of l-diethylamino-l-cyano-O-(N'- methylcarbamoyl)-formoxime and 3 parts of dichlorophenyl-tri-chloroethane are dissolved in 95 parts of kerosene.

These solutions are sprayed with pressure sprayers. The solution (a) is advantageously used for the control of leaf aphids on fruit trees and other plants. The solutions (b) and (c) are used in particular for the control of flies and mosquitoes in buildings, storerooms and slaughter houses. I

Insecticidal and acaricidal tests with the compounds of Formula I have shown that the novel l-cyano-O- carbamoyl-formoximes have a very good systemic insecticidal action; in addition, they are good to very good stomach and contact poisons. Tests of their action were made with insects of the families Muscidae, St'omoxidae and Culicidae, e.g. with polyvalent resistant and normally sensitive house flies (Musca domestica), stable flies (Stomoxys calcitrans) and mosquitoes (e.g. Aedes Aegypti, Culex fatigans, Anopheles stephensi); with insects of the families Curculionidae, Bruchididae, Dermestidae, Tenebrionidae and Chrysomelidae, e.g. granary weevils (Sitophilus granarius), beam beetles (Bruchidus obtectus), larder beetles (Dermestes vulpinus), yellow mealworms (Tenebrio molitor), Colorado potato beetles (Leptinotarsa decemlineata) and their stages of development; with insects of the family Pyralididae, e.g. Mediterranean flour moths (Ephestia kuhniella), as well as of the family Blattidae,e.g. Cockroaches (Phyllodromia germanica, Periplaneta americana, Blatta orientalis), the family Aphididae e.g. bean aphids (Aphis fabae); in addition, with insects of the family Pseudococcidae, e.g. citrus mealybugs (Planococcus citri) and of the family Locustidae, such as migratory locusts (Locusta migratoria). The tests on the said bean aphids, citrus mealybugs and migratory locusts demonstrate a systemic action.

In addition, the active substances of the Formula I according to the invention have. a good action on the larval and adult stages of spiders, e.g. of the families Acarinae, Ixodidae, Arachnidae and Argasidae.

Furthermore the active substances of Formula I have excellent nematocidal and soil-fungicidal properties.

In admixture with synergists such as succinic acid dibutyl ester, piperonyl butoxide, and auxiliaries having a similar action such as olive oil, peanut oil, etc., the range of action of the active substances according to the invention is broadened and, in particular, the insecticidal and acaricidal action is improved. In the same way, the insecticidal action can be substantially broadcried and adapted to the prevailing circumstances by the addition of other insecticides such as phosphoric, thiophosphoric and dithiophosphoric acid esters and amides, carbamic acid esters, halogenated hydrocarbons and analogues of DDT active substance, as well as pyrethrins and synergists thereof.

Systemic insecticidal action In order to determine the systemic action of the new compounds, cabbage, tomato and horsebean plants in flower pots containing 600 cc of humus are watered with 50 ml of an aqueous emulsion containing 0.48 percent of active substance (prepared from a 10 percent emulsion concentrate).

After 24 hours the parts of the plants above ground are infested with the test animals. 10 Desert locusts (Locusta migratoria, 3rd stage) are placed on each cabbage plant, 10 citrus mealybugs (Pseudococcus citri) on each tomato plant, and 10 bean aphids (Aphisfabae) on each horsebean plant. All tests are duplicated. The time elapsing until all insects are in dorsal position is determined. (Test period 3 days, ambient temperature 2530).

a. Tests with Locusta migratoria (3rd stage) time active substance elapsed (in hrs) until 100% in dorsal position l-diethylaminol-cyanoO-(N'-methylearbamoyl)- formoxime 24 l-isoprpylamino-l-cyano-O-(N'-methylcarbamoyl)- formoxime 48 l-piperidino-l-cyano-O(N'-methylcarbamoyl)- formoxim 72 l-morpholino-l -cyano-O-( N-methylcarbamoyl formoxime 24 l-methylthio-l-cyano-O-(N-methylcarbamoyl)- formoximc (known from South African Pat. No. 6616759 or the French Pat. No. l,498,899) 'no effect b. Tests with Pseudococcus citri active substance time elapsed (in hrs) until l00% in dorsal position l-m'orpholinod -c'yan o-( N '-methylcarbamoyl 24 formoxime l-isopropylaminol -cyano-O-(N '-methylcarbamoyl formoxime 72 l-methylthiol -cyano-O-( N-methylcarbamoyl )Jorm oximc (known from South African Pat. No. 66/6759 or the French Pat. No. l.498,899) no effect c. Tests with Aphis fabae activc substance time elapsed (in hrs) until 100% in dorsal position l-dicthylamino-l-cyano-O-(N'-methylcarbamoyl)- formoximc 24 I-n-propylamino-l-cyano-O-(N'-mcthylcarbamoyl)- formoxime 24 l-isopropylumino-l-cyano-O-(N'-mcthylcarbamoyl)- formoxime 24 l-n-butylaminol-cyano-O-( N -methylcarbamoyl formoximc 24 l-morpholinol -cyano-O (N '-methylcarhamoyl)- formoximc 24 l-morpholinol -cyano-O-( N'.N '-dimcthyl formoxime 24 I -pipcridino-l -cyano-O-( N -mcthylcarhamoyl t'ormoxime 24 l-methylthio-l-cyano-O-(N mcthylcarbamoyl)-formoxime (known from South African Pat. No. (16/6759 or the French Pat. No. 1,498,899) no effect Stomach poison test In order to determine the action of the new compounds as stomach poison, cabbage and potato plants in flower pots are sprayed until completely wet with an aqueous emulsion containing 0.05 percent of active substance (prepared from a 10 percent emulsion concentrate). For a first test a third of the treated plants are used-After 1 hour 10 Colorado beetle larvae (Leptinotarsa decemlineata, 3rd stage) are placed on each potato plant, and 5 desert locusts (Locusta migratoria, 3rd stage) are placed on each cabbage plant. The test is repeated with the second and third portions of the treated plants after 3 and 8 days, respectively. All tests are duplicated. The time elapsing until all insects are in dorsal position is determined. (Test period 2 days, ambient temperature 25-30).

a. Tests with Leptinotarsa decemlineata (3rd stage) Time elapsed (in hrs) until in dorsal position, when plants have been infected by insects after active substance I 3 8 hr days days l-piperidino-l-cyano-O-(N-methylcarbamoyl)formoxime -24 24 24 l-morpholinol-cyano-O-( N'-methylcarbamoyl)-formoxime' 48 48 48 I -m ethylthiol -cyano-0-( N-methylcarbamoyl)-formoxime (known from South African Pat. No. 66/6759 or the French no no no Pat. No. l,498',899 efefeffect fect fect b. Tests with Locusta migratoria (3rd stage) active substance Time elapsed in hrs) until 100% in dorsal position, when plants have been infected by Contact poison test a. Tests with cotton stainers (Dysdercus fasciatus) In order to determine the action as contact poison of the new compounds, cotton plants in flower pots are sprayed until completely wet with an aqueous emulsion containing 0.025 percent of active substance (prepared from a 10 percent emulsion concentrate). After 1 hour, the plants are infested with 10 adult cotton stainers each. All tests are duplicated. The time elapsing until all insects are in dorsal position is determined. (Test period 2 days, ambient temperature 2530).

effect b. Tests with citrus mealybugs (Pseudocoecus citri) Tomato plants infested with citrus mealybugs are sprayed until completely wet with an aqueous emulsion containing 0.025 percent of active substance (prepared from a percent emulsion concentrate). All tests are duplicated. The time elapsing until all insects are in dorsal position is determined. (Test period 2 days, ambient temperature 2530.)

active substance Time elapsed (in hrs) until l00% in dorsal position l-dieth ylaminol -cyano-O-(N-methylcarbamoyl)- formoxime 24 l-isopropylamino-l-cyano-O-(N-methylcarbamoyl)- formoxime 48 l-methylthiol -cyano-O-(N-methylcarbamoyU-formoxime (known from South African patent No. 66/6759 or the French patent No. 1,498,899 no effect Acaricidal action on Tetranychus urticae In order to determine the acaricidal properties of the new compounds, 21 test is carried out with beam leaves Concentrations (in 7r) of active substance leading to l00% mortality after 6 days active substance adults quiescent eggs stages l-diethyluminol-cyano-O-(N methylcarbamoyl)-formoxime 0.05 0.05 0.05 l-morpholino I -cyano-O-(N methylcarbamoyl)-formoxime 0.05 0.05 0.1

-Continuecl active Substance Ti active substance Concentrations (in of active elapsed substance leading to (in hrs) 5 mortality after 6 days until 100% i dorsal adults quiescent eggs position stages l-diethylamino-l-cyano-O-(N"methylcarbamoyl)formoxime 24 IO gggggg gg h gi gggxg g ggh no no gggggg methylcarbamoyn 24 South African patent No. 66/6759 or effect effect .l-tert-butylamino-l-cyano-O-(Nmethylcarbamoyl)- the French patent l'498'899) i p' f V formoxime 24 r l-piperidinol -cyano O-(N methylcarbamoyD-ftormoxtme 24 l-methylthio-l-cyano-O-(N-methylcarbamoyl)- ormoxime (known from South African patent No. 66/6759 or the Nematoclda] acuon Meloldogyne arenana French patent 1498399) no 15 The amount of active substance calculated to give concentrations for application of 0.02, 0.01, 0.005 and 0.0025 percent is thoroughly mixed with sand and subsequently mixed with humus, infested with Meloidogyne arenaria. Tomato seedlings are immediately planted in the fresh humus prepared as described above. Part of the prepared humus is stored for 8 days, and then used for planting more tomato seedlings. After a test period of 28 days the number of root knots is determined. The minimum concentration of active substance preventing the formation of root knots is given in the table.

effective concentration in '71 tomato seedlings planted on the lst day 8th day active substance l-dimethylamin'o-l-cyano-O-(N-methylcarba- Acute Toxicity (LD p.o. Rat) The test compound was applied as a single dosis to the rats of the strain Wistar CF E, of both sexes, having a medium weight of -170 g. For each dose level 5 animals were used. The rats were observed for one week after the administration of the test compounds and the number of deaths per dose level was determined.

The LD was determined by graphic interpolation from two doses actually administered, one of which killed less, the other more than half the number of animals treated. The results are given in the table below.

formoxime l-methylthio- -cyano-O-(N -methylcarbamoyl 2 formoxime (known from the South African Pat. No. 66/6759 or the French Pat. No. 1,498,899)

We claim: 1. l-Morpholino-l-O-(N,N'-dimethylcarbamoyl)- formoxime. 

